Senior QC Reviewer
Weedon, Northamptonshire (NN7)
Competitive Salary (Dependent on Experience)
Permanent | Full Time | Monday to Friday
Join a Growing Pharmaceutical Business
LM Manufacturing Limited is an FDA and MHRA-approved pharmaceutical manufacturing facility currently undergoing an exciting transformation as part of the Zydus Group, a leading global life sciences organisation.
As we continue to invest in our people, quality systems and manufacturing capabilities, we are looking for an experienced Senior QC Reviewer to join our Quality Control team.
This is an excellent opportunity for an experienced pharmaceutical laboratory professional who enjoys analytical data review, quality compliance and supporting laboratory excellence within a highly regulated GMP environment.
Why Join Us?
- Work within an FDA & MHRA-approved pharmaceutical manufacturing facility.
- Be part of a growing international pharmaceutical organisation.
- Excellent opportunities for career development and progression.
- Collaborative and supportive Quality team.
- Stable long-term career with continued investment in people and technology.
The Role
Reporting to the QC Manager, you will be responsible for reviewing analytical data, laboratory documentation and quality records to ensure compliance with GMP, Data Integrity requirements and regulatory expectations.
You will also support laboratory planning, investigations and continuous improvement activities while working closely with Quality Assurance, Production and other cross-functional departments.
Key Responsibilities
- Review analytical data generated from routine and non-routine Quality Control testing.
- Review laboratory documentation to ensure completeness, accuracy and GMP compliance.
- Support laboratory planning and coordination of QC testing activities.
- Review analytical data generated using HPLC, UPLC, UV-Visible Spectroscopy, FTIR, Karl Fischer and other analytical techniques.
- Ensure compliance with GMP, ALCOA+ Data Integrity principles and internal quality procedures.
- Support investigations relating to OOS, OOT, Deviations and CAPAs.
- Review method validation, verification and method transfer documentation.
- Support internal, customer and regulatory inspections.
- Work closely with QA, Production, Engineering and Supply Chain to ensure timely release of quality documentation.
- Drive continuous improvement initiatives within the Quality Control laboratory.
About YouEssential
- 5–8 years' experience within a pharmaceutical Quality Control laboratory.
- Previous experience as a Senior QC Reviewer, QC Analyst or QC Compliance Reviewer.
- Strong experience reviewing analytical data and laboratory documentation.
- Hands-on experience with HPLC, UPLC, UV, FTIR and Karl Fischer analysis.
- Good understanding of GMP, Data Integrity (ALCOA+), ICH guidelines and pharmaceutical regulatory requirements.
- Excellent attention to detail and strong organisational skills.
- Ability to work effectively within a cross-functional GMP environment.
Desirable
- Experience using Chromeleon, Empower or similar Chromatography Data Systems (CDS).
- Experience supporting MHRA and FDA inspections.
- Experience with analytical method validation, verification and method transfer.
- Degree in Chemistry, Pharmaceutical Sciences, Pharmacy or another relevant Life Science discipline.
Benefits
- Competitive salary based on experience.
- 21 days annual leave plus UK Bank Holidays.
- Additional annual leave based on length of service (up to 4 extra days).
- Company pension scheme.
- Paid sick leave following successful completion of probation.
- Time Off in Lieu (TOIL).
- Free on-site parking.
- GP On Demand service.
- Employee Assistance Programme.
- Ongoing training and professional development.
- Long-term career opportunities within a growing pharmaceutical organisation.
Right to Work
Applicants must have the legal right to work in the UK.
Unfortunately, we are unable to offer visa sponsorship for this position.
Apply Today
If you're passionate about pharmaceutical quality, analytical excellence and ensuring medicines meet the highest regulatory standards, we'd love to hear from you.
Join LM Manufacturing and help us deliver medicines that improve patients' lives through quality, compliance and innovation.
Pay: £28,000.00-£32,000.00 per year
Benefits:
- Company pension
- On-site parking
Work Location: In person
